# K060193: Magellan-2200 Model -2 Anesthesia Machine, Model 2

- Pathway: 510(k) (Traditional)
- Applicant: Oceanic Medical Products, Inc.
- Decided: Apr 10, 2006 after 75 days
- Product code: BSZ (Gas-Machine, Anesthesia)
- Device class: 2
- Regulation: 21 CFR 868.5160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K010613 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010613: Magellan-2200, Model 1, Oceanic Medical Products, Inc. (2001) Summary page 1.

## Indications for use
The Magellan-2200 Model-2 Anesthesia Machine is Intended for spontaneous, manually assisted or automatic ventilation of patients during anesthesia. It may be used for the delivery of gases and anesthetic vapor. It is capable of monitor/alarm functions for oxygen concentration, breathing pressure and respiratory volumes. The Magellan-2200 Model-2 Anesthesia Machine in indicated for use with spontaneous, manually assisted or automatic ventilation of patients during anesthesia. It may be used for the delivery of gases and anesthetic vapor. It is capable of monitor/alarm functions for oxygen concentration, breathing pressure and respiratory volumes.

Source page: https://510kreport.com/device/K060193
Methodology: https://510kreport.com/methodology